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A novel expression system for Gs-coupled receptors
L Catanzariti1, J M Allen, B A Hemmings
1Friedrich Miescher-Institut, Basel, Switzerland.
Abstract:
Renal epithelial cells LLC-PK1 secrete high amounts of urokinase-type plasminogen activator (uPA) when stimulated through the cAMP-signaling pathway. Here we show that this characteristic can be used to identify rapidly LLC-PK1-derived cell lines expressing heterologous receptors that couple to Gs-proteins. A genomic clone encoding the mouse beta 2 adrenergic receptor (beta 2AR) was transfected stably into LLC-PK1 cells. Drug-resistant colonies were subsequently stimulated with isoproterenol and screened for the secretion uPA activity. Positive clones displayed dose-dependent uPA activity in response to isoproterenol, specifically bound the beta 2AR-agonist iodocyanopindolol and expressed beta 2AR-mRNA. The functional coupling of beta 2AR expression to the inducible uPA gene establishes that LLC-PK1 cells can be used to assay for beta 2AR (and beta 2AR-agonist) function. Our data suggest that this system can be used for functional expression of other heterologous receptors that couple to Gs-proteins.